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A Common Missense Variant in the ATP Receptor P2X7 Is Associated with Reduced Risk of Cardiovascular Events
Genetic Variation in the EGFR Gene and the Risk of Glioma in a Chinese Han Population
Modelling the Genetic Risk in Age-Related Macular Degeneration
Clinical significance of insulin-like growth factor gene polymorphisms with survival in patients with gastrointestinal stromal tumors
CNR1 Genotype Influences HDL-Cholesterol Response to Change in Dietary Fat Intake
Association of NOD1 and NOD2 genes polymorphisms with Helicobacter pylori related gastric cancer in a Chinese population
Risk-association of CYP11A1 polymorphisms and breast cancer among Han Chinese women in Southern China
Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis
Heterogeneity in Genetic Admixture across Different Regions of Argentina
Genetic Variants of IDE-KIF11-HHEX at 10q23.33 Associated with Type 2 Diabetes Risk: A Fine-Mapping Study in Chinese Population